Viewing Study NCT06117176



Ignite Creation Date: 2024-05-06 @ 7:44 PM
Last Modification Date: 2024-10-26 @ 3:12 PM
Study NCT ID: NCT06117176
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-05-09
First Post: 2023-10-30

Brief Title: Prospective Assessment Project of AirwaY Management-related Incidents in Adult Anaesthesia Care PAPAYA III
Sponsor: Insel Gruppe AG University Hospital Bern
Organization: Insel Gruppe AG University Hospital Bern

Study Overview

Official Title: Prospective Assessment Project of AirwaY Management-related Incidents in Adult Anaesthesia Care PAPAYA III - A European Multicentre Cross-sectional Observational Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: PAPAYA-III
Brief Summary: The overall objective of the study is to evaluate and analyze major and minor incidents during airway management in adults under anaesthesia care at all study sites The patient characteristics type of airway management is recorded and if airway management-related incidents occur they are analyzed in more detail to improve patient safety in the future
Detailed Description: It is a prospective observational cross-sectional European multi-centre study collecting health-related patient data on anaesthetic airway management over three months This detects the incidence and nature of local airway management problems and assesses how they are solved This will enable the investigators to identify generalisable interventions and recommendations to further improve patients airway management to improve patient safety During the observational period the anaesthesia staff in charge will fill out a screening questionnaire for airway management for every patient undergoing anaesthesia care with airway management The investigators will extract the characteristics from the local anaesthesia record system for all patients If no event arises there are no further requirements If an event occurs the anaesthesia provider will fill out an additional form asking for more details on what happened

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
2023-01752 REGISTRY Swissethics None